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Lessons from yeast: A possible cure for Parkinson's disease?
Parkinson disease (PD) is a debilitating and lethal neurodegenerative disease, 
for which there is currently no cure. It is caused by the progressive loss of 
nerve cells that produce the chemical dopamine and is characterized by the 
accumulation of abnormal aggregates of a protein called alpha-syn in these 
dopaminergic nerve cells. Several previous studies have suggested that the 
alpha-syn aggregates contribute to PD pathology, so it is possible that an 
agent that inhibits and/or, better yet, reverses alpha-syn aggregation could 
be eventually used as a therapy for PD. Evidence to suggest that agents that 
disrupt alpha-syn aggregation might have beneficial effects in individuals 
with PD has now been provided by a team of researchers, at the Ecole 
Polytechnique Fédérale de Lausanne, Switzerland, and the University of 
Pennsylvania School of Medicine, Philadelphia, who studied a rat model of the 
disease.
In the study, it was found that a protein that yeast uses to protect itself 
from protein aggregation (there is no similar protein in mammals), called 
Hsp104, dramatically reduced both the formation of alpha-syn aggregates and 
the degeneration of neurons in the brain in a rat mdoel of PD. In vitro 
studies showed that Hsp104 not only inhibited alpha-syn aggregate formation, 
but also interacted with mammalian proteins to disassemble them. The authors 
therefore suggest that Hsp104 should be considered as a potential strategy 
for the treatment of individuals with PD, after further studies on the safety 
of introducing Hsp104 into the brain.
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TITLE: Hsp104 antagonizes alpha-synuclein aggregation and reduces dopaminergic 
degeneration in a rat model of Parkinson disease
AUTHOR CONTACT: 
Patrick Aebischer 
Ecole Polytechnique Fédérale de Lausanne, Lausanne, Switzerland. 
Phone: 41-21-693-9505; Fax: 41-21-693-9510; E-mail: [log in to unmask]
James Shorter 
University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, 
USA. Phone: (215) 573-4256; Fax: (215) 
573-4764; E-mail: [log in to unmask]

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